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See other ATP5L2 GT Assays ›
SNP ID:
rs916321
Gene
ATP5L2 CYB5R3
Gene Name
Set Membership:
> HapMap > Validated
Chromosome Location:
Chr.22: 42645385 - 42645385 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

AGAGCCCAGACTCCTGGATGAGGGC[A/G]CGGCACAGCCTGTCCTGTTTGTCAG

Assay ID C___2986231_1_
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
Online offer:
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 613213

Literature Links:

 ATP5L2 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
A (0.30)
(0.70)
Caucasian
A (0.39)
(0.61)
CEPH (CEU)
A (0.36)
(0.64)
EAS
A (0.27)
(0.73)
African American
A (0.13)
(0.87)
YRI (Yoruba)
A (0.18)
(0.82)
SAS
A (0.41)
(0.59)
Chinese - Not Available JPT (Japanese)
A (0.33)
(0.67)
AFR
A (0.13)
(0.87)
Japanese - Not Available CHB (Han Chinese)
A (0.34)
(0.66)
EUR
A (0.36)
(0.64)
AMR
A (0.42)
(0.58)
ATP5L2 - ATP synthase, H+ transporting, mitochondrial Fo complex subunit G2
There are no transcripts associated with this gene.
CYB5R3 - cytochrome b5 reductase 3
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_000398.6 Intron NP_000389.1
NM_001129819.2 Intron NP_001123291.1
NM_001171660.1 Intron NP_001165131.1
NM_001171661.1 Intron NP_001165132.1
NM_007326.4 Intron NP_015565.1

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